Bard Access Systems, Inc.
1,555 devices · 34,969 adverse event reports · 271 deaths reported · 372 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- Site~Rite 8 Ultrasound System 9770601Transducer, ultrasonic, diagnostic103 reports
- BD Intraosseous Vascular Access System D015551NKNeedle, hypodermic, single lumen2 recalls1 death3 reports
- Sherlock 9770352Catheter, intravascular, therapeutic, long-term greater than 30 days102 reports
- BD Intraosseous Vascular Access System D015351NKNeedle, hypodermic, single lumen2 recalls2 reports
- DuoGlide catheter 5625240CATHETER, HEMODIALYSIS, NON-IMPLANTED2 recalls1 report
- PowerPICC SOLO CK000586BCatheter, intravascular, therapeutic, long-term greater than 30 days2 recalls1 report
- Power-Trialysis Alphacurve catheter 5655120CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls0 reports
- Power-Trialysis catheter 5615120CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls0 reports
- Power-Trialysis catheter 5605300CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls0 reports
- Power-Trialysis Slim-Cath catheter 5855300CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls0 reports
- Power-Trialysis Slim-Cath catheter 5865120CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls0 reports
- Power-Trialysis Slim-Cath catheter 5865200CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls0 reports
- Power-Trialysis Slim-Cath catheter 5865240CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls0 reports
- PowerPICC SOLO CK001030Catheter, intravascular, therapeutic, long-term greater than 30 days2 recalls0 reports
- Port Access Needle LH-0033Set, administration, intravascular1 recall49 reports
- PowerPICC Provena S1173108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall45 reports
- Per-Q-Cath Plus Catheter 4134115Catheter,intravascular,therapeutic,long-term greater than 30 days94 reports
- PowerPICC Provena S1294108D4Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall44 reports
- Guidewire 5583705WIRE, GUIDE, CATHETER1 recall43 reports
- BD Prevue II Peripheral Vascular Access System 9770703System, image processing, radiological93 reports
- Hickman 0600620Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall40 reports
- PowerPICC Provena SOLO S1395108D5Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall39 reports
- BardPort M.R.I., Groshong 0602833PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR88 reports
- PowerPICC Catheter with Sherlock 3CG Tip Positioning System (TPS) Stylet 1385108QDCatheter,intravascular,therapeutic,long-term greater than 30 days88 reports
- Port Access Needle 0131975Set, administration, intravascular1 recall38 reports
- PinPoint 9A10000Media,coupling,ultrasound88 reports
- PowerPort ClearVUE 5668362PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 recall38 reports
- PowerPICC Provena S1385108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall38 reports
- Port Access Needle 0132010Set, administration, intravascular1 recall37 reports
- Port Access Needle 0142010Set, administration, intravascular1 recall37 reports
- Port Access Needle 0632034Set, administration, intravascular87 reports
- PowerPort ClearVUE 1668362PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 recall1 death37 reports
- PowerPort, ChronoFlex 1708060PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR4 deaths86 reports
- Midline Catheter Kit S4153108BDPMidline catheter1 recall36 reports
- PowerPICC Provena S1294108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall34 reports
- Broviac 0600060Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 death33 reports
- Port Access Needle LH-0032Set, administration, intravascular1 recall33 reports
- PowerPort ClearVUE 1678300PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 recall1 death32 reports
- Midline Catheter Kit S4153108DMidline catheter1 recall32 reports
- PowerPICC Provena SOLO S1395108D2Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall32 reports
- HemoSplit Long-Term Hemodialysis Catheter 5733690Catheter, hemodialysis, implanted81 reports
- PowerPICC SV Catheter 1274108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall30 reports
- Broviac 0601620Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall29 reports
- BD SiteRite 9 Ultrasound System 9770803Transducer, ultrasonic, diagnostic79 reports
- BardPort M.R.I. 0603880PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR78 reports
- Port Access Kit 2142075Set, administration, intravascular1 recall28 reports
- Site~Rite 8 Ultrasound System 9770602YTransducer, ultrasonic, diagnostic78 reports
- PowerPICC Provena SOLO S1395108D3Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall28 reports
- PowerPICC Provena S1173108D4Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall28 reports
- Port Access Needle 012034NYSet, administration, intravascular77 reports
- PowerPICC Provena SOLO S1395108D4Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall27 reports
- PowerPICC Catheter 3174155Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall26 reports
- PowerPICC SOLO 1194108D2Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall26 reports
- PowerPICC Provena S1294108D2Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall26 reports
- PowerPICC Provena S1294108D5Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 death26 reports
- PowerPort ClearVUE 5618000PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR5 deaths75 reports
- PowerPICC SOLO2 Catheter 3194355Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall25 reports
- Niagara Slim-Cath catheter 5553200CATHETER, HEMODIALYSIS, NON-IMPLANTED75 reports
- Port Access Needle 0142275Set, administration, intravascular1 recall25 reports
- PowerLine 0700615Catheter,intravascular,therapeutic,long-term greater than 30 days2 deaths74 reports
- Port Access Needle LH-0037Set, administration, intravascular1 recall24 reports
- PowerPICC SOLO 1194108D3Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall24 reports
- PowerPort ClearVUE 1606062PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR3 deaths73 reports
- PowerPort ClearVUE 1608052PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 death73 reports
- PowerPICC Provena S9274108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall23 reports
- PowerPort M.R.I. 1809600PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 death72 reports
- Groshong Catheter 7715405CATHETER, PERCUTANEOUS72 reports
- Port Access Needle 0141975Set, administration, intravascular1 recall22 reports
- PowerPICC Provena S1385108D4Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall22 reports
- PowerPort M.R.I., ChronoFlex 1808001PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR6 deaths69 reports
- PowerPICC SOLO2 Catheter 3194335Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall18 reports
- PowerPICC SOLO2 Catheter with Sherlock Tip Location System (TLS) Stylet 9194118Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall18 reports
- PowerPICC® SV Catheter 3173355Catheter,intravascular,therapeutic,long-term greater than 30 days67 reports
- Navarre Opti-Drain NOD12LPTCATHETER, IRRIGATION67 reports
- Port Access Needle 0131910Set, administration, intravascular1 recall17 reports
- Port Access Needle 0652034Set, administration, intravascular67 reports
- Peripheral Catheter Insertion Kit F118100Catheter,intravascular,therapeutic,short-term less than 30 days67 reports
- PowerPort ClearVUE 1616070PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR66 reports
- Port Access Needle 0672034Set, administration, intravascular66 reports
- PowerPort ClearVUE 1676300PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 recall16 reports
- BardPort, Groshong 0606150PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR65 reports
- PowerPort M.R.I., ChronoFlex 4808060PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR2 deaths65 reports
- PowerPICC® Catheter 3174335Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall15 reports
- PowerPICC Catheter with Sherlock 3CG Tip Positioning System (TPS) Stylet 1174108Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall15 reports
- PowerLine 0700515Catheter,intravascular,therapeutic,long-term greater than 30 days65 reports
- Power-Trialysis catheter 5605200CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 recall1 death15 reports
- Midline Catheter Kit S4153108DGPMidline catheter1 recall15 reports
- BardPort M.R.I. 0604580PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR64 reports
- Broviac 0600040Catheter,intravascular,therapeutic,long-term greater than 30 days64 reports
- Port Access Needle 012001NYSet, administration, intravascular64 reports
- Port Access Needle LH-0035YNSet, administration, intravascular1 recall14 reports
- PowerPICC CK000775ACatheter, intravascular, therapeutic, long-term greater than 30 days1 recall14 reports
- HemoSplit Long-Term Hemodialysis Catheter 5733730Catheter, hemodialysis, implanted1 death63 reports
- Groshong NXT Catheter 7927505Catheter,intravascular,therapeutic,long-term greater than 30 days63 reports
- Port Access Needle LH-0030Set, administration, intravascular1 recall13 reports
- PowerPICC 1174108D2Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall13 reports
- PowerPICC Provena S1193108D5Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall13 reports
- PowerPICC Catheter 3174355Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall12 reports
- Hickman 0601680Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall12 reports
- Hickman 0601760Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall12 reports